Nuclear factor κB mutations in human subjects: The devil is in the details-Reference-Cited by-同舟云学术

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Nuclear factor κB mutations in human subjects: The devil is in the details

Published:2018-10 Issue:4 Volume:142 Page:1062-1065
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Fliegauf Manfred,Grimbacher Bodo

Funder

German Ministry of Education and Research

E-rare program of the European Commission EURO-CMC

German Center for Infection Research

Deutsche Forschungsgemeinschaft

Bristol-Myers Squibb

CSL Behring

Novartis

Baxalta

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference11 articles.

1. Human NF-κB1 haploinsufficiency and Epstein-Barr virus-induced disease-molecular mechanisms and consequences;Hoeger;Front Immunol,2018

2. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans;Tuijnenburg;J Allergy Clin Immunol,2018

3. Aberrant NF-κB signaling in lymphoma: mechanisms, consequences, and therapeutic implications;Jost;Blood,2007

4. Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes;Kaustio;J Allergy Clin Immunol,2017

5. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO);Zonana;Am J Hum Genet,2000

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1. Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis;Cell Reports Medicine;2024-04

2. Interplay between epigenetic and genetic alterations in inborn errors of immunity;Trends in Immunology;2023-11

3. Integrated Multi-omics Analyses of NFKB1 patients B cells points towards an up regulation of NF-κB network inhibitors;2022-11-23

4. Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations;Frontiers in Immunology;2022-09-20

5. Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50;Frontiers in Immunology;2022-08-29

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